Identification and characterization of a human cDNA and gene encoding a ubiquitously expressed glucose-6-phosphatase catalytic subunit-related protein.
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Functional analysis of mutations in a severe congenital neutropenia syndrome caused by glucose-6-phosphatase-β deficiencyG6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunctionFoxa2 and MafA regulate islet-specific glucose-6-phosphatase catalytic subunit-related protein gene expressionA syndrome with congenital neutropenia and mutations in G6PC3Glycogen metabolism in humansHistidine 167 is the phosphate acceptor in glucose-6-phosphatase-beta forming a phosphohistidine enzyme intermediate during catalysisGlucose-6-phosphatase catalytic subunit gene familyGlycogen storage disease type I and G6Pase-β deficiency: etiology and therapyA potential new role for muscle in blood glucose homeostasisIdentification and characterisation of a new human glucose-6-phosphatase isoformSevere congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis.A potential role for muscle in glucose homeostasis: in vivo kinetic studies in glycogen storage disease type 1a and fructose-1,6-bisphosphatase deficiencyMoving on from GWAS: functional studies on the G6PC2 gene implicated in the regulation of fasting blood glucose.Multi-tissue computational modeling analyzes pathophysiology of type 2 diabetes in MKR mice.Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels.The islet-specific glucose-6-phosphatase-related protein, implicated in diabetes, is a glycoprotein embedded in the endoplasmic reticulum membrane.Dynamics of intra-follicular glucose during luteinization of macaque ovarian folliclesAdult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotypeCerebral Gluconeogenesis and Diseases.Silencing of the human microsomal glucose-6-phosphate translocase induces glioma cell death: potential new anticancer target for curcumin.Specific reduction of hepatic glucose 6-phosphate transporter-1 ameliorates diabetes while avoiding complications of glycogen storage disease.A detailed characterization of the adult mouse model of glycogen storage disease Ia.Novel stable isotope analyses demonstrate significant rates of glucose cycling in mouse pancreatic islets.Glycans Instructing Immunity: The Emerging Role of Altered Glycosylation in Clinical Immunology.Genetic and functional assessment of the role of the rs13431652-A and rs573225-A alleles in the G6PC2 promoter that are strongly associated with elevated fasting glucose levels.The stages of type 1A diabetes: 2005.Functional Analysis of Mouse G6pc1 Mutations Using a Novel In Situ Assay for Glucose-6-Phosphatase Activity and the Effect of Mutations in Conserved Human G6PC1/G6PC2 Amino Acids on G6PC2 Protein Expression.Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage diseaseNeutropenia in primary immunodeficiencyThe Effects of Myo-Inositol and B and D Vitamin Supplementation in the db/+ Mouse Model of Gestational Diabetes MellitusType I glycogen storage diseases: disorders of the glucose-6-phosphatase/glucose-6-phosphate transporter complexes.Hepatocyte nuclear factor-4 alpha mediates the stimulatory effect of peroxisome proliferator-activated receptor gamma co-activator-1 alpha (PGC-1 alpha) on glucose-6-phosphatase catalytic subunit gene transcription in H4IIE cells.Hepatocytes contribute to residual glucose production in a mouse model for glycogen storage disease type Ia.Sequence variation between the mouse and human glucose-6-phosphatase catalytic subunit gene promoters results in differential activation by peroxisome proliferator activated receptor gamma coactivator-1alphaThe pancreatic islet β-cell-enriched transcription factor Pdx-1 regulates Slc30a8 gene transcription through an intronic enhancer.The three insulin response sequences in the glucose-6-phosphatase catalytic subunit gene promoter are functionally distinct.A glucose-6-phosphate hydrolase, widely expressed outside the liver, can explain age-dependent resolution of hypoglycemia in glycogen storage disease type Ia.Selective stimulation of G-6-Pase catalytic subunit but not G-6-P transporter gene expression by glucagon in vivo and cAMP in situ.Deletion of the gene encoding the ubiquitously expressed glucose-6-phosphatase catalytic subunit-related protein (UGRP)/glucose-6-phosphatase catalytic subunit-beta results in lowered plasma cholesterol and elevated glucagon.Liver glyconeogenesis: a pathway to cope with postprandial amino acid excess in high-protein fed rats?
P2860
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P2860
Identification and characterization of a human cDNA and gene encoding a ubiquitously expressed glucose-6-phosphatase catalytic subunit-related protein.
description
2002 nî lūn-bûn
@nan
2002 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Identification and characteriz ...... lytic subunit-related protein.
@ast
Identification and characteriz ...... lytic subunit-related protein.
@en
Identification and characteriz ...... lytic subunit-related protein.
@nl
type
label
Identification and characteriz ...... lytic subunit-related protein.
@ast
Identification and characteriz ...... lytic subunit-related protein.
@en
Identification and characteriz ...... lytic subunit-related protein.
@nl
prefLabel
Identification and characteriz ...... lytic subunit-related protein.
@ast
Identification and characteriz ...... lytic subunit-related protein.
@en
Identification and characteriz ...... lytic subunit-related protein.
@nl
P2093
P356
P1476
Identification and characteriz ...... lytic subunit-related protein.
@en
P2093
P304
P356
10.1677/JME.0.0290205
P577
2002-10-01T00:00:00Z